A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046254



Internal ID18788785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46176448..46257987hg38UCSC Ensembl
Innerchr10:47547684..47629223hg19UCSC Ensembl
Innerchr10:47017690..47099229hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3881540
hg1981540
hg1881540
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv830n100
Supporting Variantsnssv3512762
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046254
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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